A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13694574



Internal ID21216425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60365043..60365043hg38UCSC Ensembl
chr15:60657242..60657242hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2794976
Supporting Variants
Samples
Known GenesANXA2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13694574
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.419355


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